A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606622



Internal ID16394031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37535065..37564925hg38UCSC Ensembl
Innerchr7:37574668..37604528hg19UCSC Ensembl
Innerchr7:37541193..37571053hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3829861
hg1929861
hg1829861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1082702
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606622
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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